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儿童噬血细胞综合征10例临床分析

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摘要 目的探讨HLH-2004方案诊治噬血细胞综合征(HLH)的效果,分析HLH的相关病因。方法 10例(男6例、女4例)HLH患儿,平均年龄2.5岁。按HLH-2004方案进行诊断和治疗,并进行可能的病因检查和分析其相关病因。结果 10例中6例(60%)与感染相关,2例(20%)与非感染相关,2例(20%)病因不明。按HLH-2004方案诊断和治疗,1例在治疗过程中死于消化道出血,9例早期均能获得缓解,5例完成治疗在随访中。结论 HLH-2004方案有较强的诊断可行性、治疗可获得早期缓解。
出处 《当代医学》 2010年第33期65-66,共2页 Contemporary Medicine
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参考文献3

  • 1Henter JI,Home A,Aric ó M.et al.HLH-2004:diagnostic and therapeutic guidelines for hemophagoocytic lymphohistiocytos[J].Pediatr Blood Cancer,2007,48(2):124-131.
  • 2汤永民.加强儿童噬血细胞综合征的早期诊断与干预研究[J].临床儿科杂志,2009,27(8):705-708. 被引量:10
  • 3Lay JD,Chuang SE,Rowe M,et al.Epstein-barr virus latent membrane protein-1 mediates upregulation of tumor necrosis factor-alpha in EBV infected T cells:implications for the pathogenesis of hemophagocytic syndrome[J].J Biomed sci,2003,10(1):146-155.

二级参考文献18

  • 1汤永民,廖婵.噬血细胞综合征的分子生物学基础及其发病机制[J].实用儿科临床杂志,2006,21(9):513-516. 被引量:11
  • 2Farquhar JW, Claireaux AE. Familial haemophagocytic reticulosis [J]. Arch Dis Child, 1952,27(136) :519-525.
  • 3Menasche G, Feldmann J, Fischer A, et al. Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis [J]. Immunol Rev, 2005,203 : 165-179.
  • 4Toitt I, Brostoff J, Male D. Immnulogy [M]. 6th ed. Harcourt Publishers Limited, 2001 : 235-258.
  • 5Stepp SE, Dufourcq-Lagelouse R, Le Deist F, et al. Perforin gene defects in familial hemophogocytic lympho- histiocytosis [J]. Science, 1999,286(5446) : 1957-1959.
  • 6Katano H, Cohen JI. Pefforin and lymphohistiocytic proliferative disorders [ J ]: Br J Haematol, 2005,128 (6) : 739- 750.
  • 7Zur Stadt U, Beutel K, Kolberg S, et al. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STXII, and RAB27A [J]. Hum Mutat, 2006,27(1) :62-68.
  • 8Feldmann J, Callebaut I, Raposo G, et al. Muncl3-4 is essential for eytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistioeytosis (FHL3) [J]. Cell,2003,115(4) :461-473.
  • 9Yamamoto K, Ishii E, Sako M, et al. Identification of novel MUNC13-4 mutations in familial haemophagocytic lym-phohistiocytosis and functional analysis of MUNC13- 4-deficient cytotoxic T lymphocytes[J].J Med Genet, 2004,41 (10) :763-767.
  • 10zur Stadt U, Schmidt S, Kasper B, et al. Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11[J]. Hum Mol Genet,2005,14(6) :827-834.

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